書名 | 作者 | 出版年 | 查看 | 回報錯誤連結 |
Equipment qualification in the pharmaceutical industry |
Steven Ostrove. |
2019 |
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Continuous manufacturing of pharmaceuticals |
Peter Kleinebudde, Johannes Khinast, Jukka Rantanen. |
2017 |
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Handbook of pharmaceutical granulation technology |
Dilip M. Parikh. |
2010 |
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Testing computer systems for FDA/MHRA compliance |
David Stokes. |
2004 |
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Pharmaceutical powder compaction technology |
|
2011 |
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Pharmazeutische mikrobiologie:qualitätssicherung, monitoring, betriebshygiene / |
Michael Rieth. |
2012 |
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Isolation technology:a practical guide / |
Tim Coles. |
2004 |
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Quality control training manual:comprehensive training guide for API, finished pharmaceutical and biotechnologies laboratories / |
Syed Imtiaz Haider, Erfan Asif Syed. |
2011 |
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Handbook of isolation and characterization of impurities in pharmaceuticals |
Satinder Ahuja, Karen Mills Alsante. |
2003 |
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Structure and chemistry |
Vijay Kumar Thakur and Manju Kumari Thakur. |
2015 |
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回報問題連結 |
Processing and applications |
Vijay Kumar Thakur and Manju Kumari Thakur. |
2015 |
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回報問題連結 |
How to develop robust solid oral dosage forms :from conception to post-approval / |
Bhavishya Mittal. |
|
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回報問題連結 |
Human vaccines :emerging technologies in design and development / |
Kayvon Modjarrad, MD, PhD, Wayne C. Koff, PhD. |
|
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回報問題連結 |
Sterile drug products:formulation, packaging, manufacturing, and quality / |
Michael J. Akers. |
2010 |
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回報問題連結 |
An introduction to pharmaceutical sciences:production, chemistry, techniques and technology / |
Jiben Roy. |
2011 |
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回報問題連結 |
Novel approaches and strategies for biologics, vaccines and cancer therapies |
Manmohan Singh, Maya Salnikova. |
©2015 |
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